21 research outputs found
Role of Periaxin dimerization in peripheral myelination
- Author
- Publication venue
- The University of Edinburgh
- Publication date
- 22/06/2012
- Field of study
In the peripheral nervous system (PNS), Schwann cells ensheathe and myelinate
axons to promote saltatory conduction of nerve impulses. Close interactions between
Schwann cells and axons, and Schwann cells and the basal lamina are essential for
the regulation of Schwann cell development and function. Myelinating Schwann
cells are highly polarized radially and longitudinally for specifying distinct domains
in the axon, which is required for fast action potential propagation. In addition, the
Schwann cell cytoplasm is organized into discrete compartments, called Cajal bands,
which contain different dystrophin-glycoprotein complexes that are believed to
segregate the Schwann cell plasma membrane into appositions between the outer
surface of the myelin sheath and the cytoplasmic face of the Schwann cell plasma
membrane.
Periaxin is expressed in myelinating Schwann cells, and homodimerizes at its
PDZ domain to form a transmembrane complex with dystrophin-related protein 2
(DRP2) and dystroglycan. This PDG complex is concentrated at the appositions, and
is essential for myelin sheath maintenance and stability in the mature PNS. In mice
lacking Periaxin, an intact myelin sheath is formed but subsequently becomes
unstable. Periaxin-null Schwann cells are also shorter, which has been proposed to
result in a reduction in nerve conduction velocity.
This thesis is a study of how Periaxin PDZ domain dimerization contributes
to the regulation of PDG complex stability, apposition maintenance, Schwann cell
internodal distance and myelin stability. I have studied the function of Periaxin by
generating a conditional mutant mouse that lacks the PDZ domain, which is
predicted to abrogate dimerization. In these mutants, DRP2 is severely depleted and
appositions containing DRP2 fail to form. Mutant Schwann cells also have disrupted
Cajal bands and shorter internodal lengths. In the mature peripheral nerves, mutant
mice display a peripheral neuropathy characterized by hypermyelination with focally
folded myelin. Nerve conduction velocity, motor coordination and sensory function
were also studied in these mutant mice. Taken together, these data suggest that
dimerization of the Periaxin PDZ domain is required for the stabilization of the PDG
and appositions, and regulation of Schwann cell elongation and myelin maintenance.
By analyzing a tamoxifen-inducible conditional mouse lacking Periaxin’s
PDZ domain in mature myelinating Schwann cells, this work also shows that
Periaxin dimerization is essential for maintaining Schwann cell
compartmentalization and myelin stability in adult nerves.
Finally, studies of single amino acid mutations of the Periaxin PDZ reveal
that subtle changes in the structure of the PDZ domain can abrogate dimerization,and a possible mechanism for PDZ-PDZ homodimerization of Periaxin is proposed
Single-cell multiomics identifies clinically relevant mesenchymal stem-like cells and key regulators for MPNST malignancy
- Publication venue
- Digital Commons@Becker
- Publication date
- 04/11/2022
- Field of study
Malignant peripheral nerve sheath tumor (MPNST), a highly aggressive Schwann cell (SC)-derived soft tissue sarcoma, arises from benign neurofibroma (NF); however, the identity, heterogeneity and origins of tumor populations remain elusive. Nesti
Robust estimation of bacterial cell count from optical density
- Author
- Aarnio Tiu
- Aaron Leow Chung Yong
- Abbas Anser
- Abduraimova Aiganym
- Abraham Doris
- Acar Beliz Leyla
- Acosta Joaquin
- Adler Nina
- Adulyanukosol Natthawut
- Agena Ejouan
- Agena Ethan
- Aggarwal Priya
- Aguirre Adriana Lizeth Rubio
- Ahlgren Christopher
- Ahuja Janvi
- Aizik Dror
- Akbary Mina
- Akinfenwa Akinwumi
- Akingbesote Ngozi D.
- Akova Umut
- Aldo Ferdinan
- Alexopoulos Ioannis
- Allen Lucy
- Alonso Alejandro
- Altarawneh Dina
- Alvarado Andres Benjamin Sanchez
- Ambre Sanika
- Ameziane Annissa
- Amheine Khadija
- Amin Ihya Fakhrurizal
- Amir Sayeda Sakina
- Amstel Chiel van
- An Yongyan
- Anand Nithishwer Mouroug
- Ananthakrishnan Sathvik
- Anderson Karl
- Angel Sagi
- Annem Vidhya
- Anson Chung Tsun Ho
- Anwar Mariam
- Appel Alana
- Araya Lucas
- Armstrong Alexander
- Arora Neha
- Arora Vasu
- Arruda Beck
- Ashwin F Amal Jude
- Astapenka Artur
- Astles Ben
- Astorino Gabe
- Aubry Celine
- Avileli Rebecca
- Azad Mahnaz Sabeta
- Babar Rehmat
- Babu Priyanka
- Badalli Turan
- Badash Lior
- Baichman-Kass Amichai
- Baldwin Geoff S.
- Baltensperger Oliver Andreas
- Bao Guanke
- Bao Minyue
- Baronaite Ugne
- Barrat Leon Michael
- Barrington Seth
- Barshap Alon
- Bartzoka Natalia
- Basu Anubhav
- Basulto Cynthia
- Bath Scott
- Battina Rohith
- Bauersachs Daniel
- Beal Jacob
- Beale Renee
- Beard Eleanor
- Beck Selina
- Becker Evan
- Benavides Samantha Ayde Pena
- Bennis Nicole
- Bete Anna
- Bhatt Darshak
- Bhowmick Shilpa
- Bian Weixin
- Bijman Eline Yafele
- Bindt Felix
- Blas Karla Soto
- Bo Tang
- Boada Yadira
- Boer Meine
- Bohner Ariel
- Borovko Irina
- Bott Amie
- Bouwmeester Susan
- Bowman Kyle
- Boxem Mike
- Boxuan Cheng
- Boyce Kira
- Boyer Jess
- Brasas Valentas
- Brewer Mathew
- Briand William
- Brink Matilda
- Browne Emily
- Buckley-Taylor Russell
- Budhan Stephanie
- Buller Lisa
- Burckhardt Nele
- Burgland Zachary
- Burns Frank
- Burridge Matt
- Burud Hanna Nedreberg
- Buson Felipe Xavier
- Butterfield Tom
- Byagathvalli Gaurav
- Byatt Gabriel
- Byun Sumin
- Caballero Amalia
- Cai Fu
- Cai Niangui
- Caldwell Sarah
- Camacho Yazmin
- Camille Monteil
- Campbell Robert
- Cao Qinhao
- Cao Yixin
- Cao Yuze
- Carrillo Leo
- Carter Jonah
- Casas Alexis
- Castillo Nora Esther Torres
- Castillo Sandra
- Cave John
- Chai Ruochen
- Chamiec-Case Elizabeth
- Chan Janice
- Chan Yuan-Yao
- Chandramouli Priyanka
- Chang Annabel
- Chang Catherine
- Chang Kevin
- Chang Thomas
- Chang Ting-Chen
- Chang Yu-Ci
- Chapman Tyler
- Chater Dounia
- Chau Anthony
- Chavez Benjamin
- Chavez Francisco
- Chehade Ibrahim
- Chen Carmen
- Chen Chih-Chiang
- Chen Ching-Wei
- Chen Janice
- Chen Junhong
- Chen Junyang
- Chen Junyu
- Chen Pei-Hong
- Chen Ryan
- Chen Weixuan
- Chen Yan
- Chen Yi-Cian
- Chen Yifei
- Chen Zhuoyang
- Cheng Cheng
- Cheng Haolun
- Cheng Hsuan
- Cheng Yu-Hong
- Cheng Yu-Hsuan
- Chenxi Liang
- Cherupalla Arjun
- Chi Jordi
- Chi Shumei
- Chiang Jason
- Chiang Woody
- Ching Lai Tsz
- Ching Lam Kai
- Ching Law Hiu
- Ching Luk Hau
- Chinnathambi Sathivel
- Cho Sungwoo
- Choi Lee Sze
- Choi Youngeun
- Chou Ryan
- Chou Ryan
- Chu Wai Yan
- Chua Yah Tse Sabrina
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- Chulkova Nadezhda
- Chun Cheung Man
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- Cifuentes Rodrigo Hernandez
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- Clodomir Christina
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- Craw Darilyn
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- Crowley Peter
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- Cubukcu Hande
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- Czekster Clarissa
- Dai Leijie
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- Das Neves Laura
- Das Diptatanu
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- De Silva Nimaya
- Deb Shalini S.
- Deepak Kumar S.
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- Dirven Yvette
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- Dominguez Viana Isabel Perez
- Dong Dongyang
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- Dong Shangzhi
- Doyle David
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- Dunstan Izzy
- Dusseaux Theodore A.
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- Edelmayer Marco
- Ehrenworth Amy
- Eidloth Franziska
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- El Moubayed Yorgo
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- Emilov Kristian
- Espinoza Diego
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- Gokul [NO FIRST NAME IN SCOPUS]
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- Zhang Yunqian
- Zhang Zixuan
- Zhao Nannan
- Zhao Peng
- Zhao Tianyan
- Zhao Wenxue
- Zhao Yihang
- Zhaoting Li
- Zhecheng Huang
- Zheng Daniel
- Zheng Jiyang
- Zhiwei Song
- Zhong Yanling
- Zhou Hanmi
- Zhou Jiajie
- Zhou Jianan
- Zhou Rui
- Zhou Shuyao
- Zhou Xuanhao
- Zhou Yanjun
- Zhou Yi
- Zhou Yinchi
- Zhou Yineng
- Zhou Yuezhang
- Zhou Yuxin
- Zhou Zhiyu
- Zhu Chushu
- Zhu Ke
- Zhu Xueqian
- Zi Lihan
- Zilinskaite Nemira
- Zimmermann Andreas
- Zimmermann Jennifer
- Zirong Zeng
- Ziwei Zhou
- Ziyi Zhao
- Zorrilla Francisco
- Zou Jiahua
- Zukauskaite Kristina
- Zulueta Patricia
- Zvirblyte Justina
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data
New genetic loci link adipose and insulin biology to body fat distribution.
- Author
- Aalto Ville
- Aasarød Knut
- Abecasis Goncalo R
- Abecasis Gonçalo
- Absher Devin
- Adair Linda S
- Adam Martin
- Adeyemo Adebowale
- Ahlqvist Emma
- Ahmadi Kourosh R
- Ahola Aila
- Ainali Chrysanthi
- Akylbekova Ermeg
- Ala-Korpela Mika
- Alavere Helen
- Albagha Omar M E
- Albrecht Eva
- Alen Markku
- Alexander Myriam
- Alhenc-Gelas François
- Alizadeh Behrooz Z
- Allison Matthew A
- Alonso Nerea
- Altshuler David
- Ambite Jose Luis
- Amin Najaf
- Amouyel Philippe
- An Ping
- Anderson Carl A
- Anderson Denise
- Anderson Garnet
- Andrews Jeanette S
- Antonella Mulas
- Antti Jula
- Aragaki Aaron K
- Arking Dan E
- Arnold Alice
- Arnold Alice M
- Arora Pankaj
- Arscott Gillian M
- Artigas Maria Soler
- Arveiler Dominique
- Asiki Gershim
- Aspelund Thor
- Assimes Themistocles L
- Atalay Mustafa
- Atkinson Elizabeth J
- Aulchenko Yurii
- Avery Christy
- Bain Stephen C
- Bakker Stephan J L
- Balcells Susana
- Balkau Beverley
- Ballantyne Christie M
- Balmforth Anthony J
- Bandinelli Stefania
- Barbalic Maja
- Barrett Amy
- Barroso Ines
- Barroso Inês
- Basart Hanneke
- Basart Hanneke V
- Bataille Veronique
- Baumert Jens
- Beckmann Jacques S
- Beekman Marian
- Been Latonya F
- Beilby John
- Beilby John P
- Bell Jordana T
- Bellis Claire
- Bennett Amanda J
- Bennett Franklyn
- Berenson Gerald S
- Bergman Richard N
- Bergmann Sven
- Berndt Sonja I
- Berne Christian
- Bidulescu Aurelian
- Bielak Lawrence F
- Bierut Laura J
- Biffar Reiner
- Bis Joshua C
- Blackburn Hannah
- Blangero John
- Blankenberg Stefan S
- Blüher Matthias
- Boban Mladen
- Bochud Murielle
- Boehm Bernhard O
- Boehnke Michael
- Boerwinkle Eric
- Boezen H Marike
- Bolton Jennifer L
- Bolton Judith A Hoffman
- Bonnet Fabrice
- Bonnycastle Lori L
- Boomsma Dorret I
- Borecki Ingrid
- Boright Andrew P
- Borja Judith B
- Bornstein Stefan R
- Boston Jonathan
- Bots Michiel L
- Bouatia-Naji Nabila
- Bouchard Claude
- Bovet Pascal
- Boyd Heather A
- Bragg-Gresham Jennifer L
- Brambilla Paolo
- Brand Eva
- Brand Stefan-Martin
- Brandi Maria Luisa
- Braund Peter S
- Brennan Eoin P
- Brismar Kerstin
- Brody Jennifer
- Broekmans Frank J
- Broer Linda
- Brown Matthew A
- Brown Morris J
- Brown-Gentry Kristin
- Bruinenberg Marcel
- Buchkovich Martin L
- Buckley Brendan M
- Buil Alfonso
- Bull Shelley B
- Burgdorf Christof
- Buring Julie E
- Burnett Mary S
- Burnier Michel
- Burri Andrea
- Burton Paul R
- Bush William S
- Busonero Fabio
- Buxbaum Sarah G
- Buyske Steve
- Buzkova Petra
- Byrne Enda M
- Böger Carsten A
- Böhringer Stefan
- Böttcher Yvonne
- Cambien Francois
- Campbell Harry
- Campbell Susan
- Carba Delia B
- Carlson Chris
- Carlson Olga D
- Carty Cara
- Casas Juan P
- Caspersen Ida H
- Castano-Betancourt Martha
- Cauchi Stéphane
- Cauley Jane A
- Caulfield Mark
- Cavalieri Margherita
- Cazier Jean-Baptiste
- Center Jacqueline R
- Cesana Giancarlo
- Chakravarti Aravinda
- Chambers John
- Chandak Giriraj R
- Chang Hsing-Yi
- Chang Yen-Pei C
- Chanock Stephen J
- Charchar Fadi J
- Chasman Dan
- Chaturvedi Nish
- Chen Constance
- Chen Han
- Chen Ida
- Chen Jin
- Chen Ming-Huei
- Chen Wei
- Chen Yii-Der Ida
- Cheng Iona
- Cheng Sulin
- Chines Peter S
- Cho Yoon Shin
- Choi Murim
- Chouraki Vincent
- Christiansen Claus
- Chu Audrey Y
- Cimponeriu Dan
- Ciullo Marina
- Clark Graeme R
- Clarke Robert
- Claudi-Boehm Simone
- Coassin Stefan
- Cochran Barbara
- Cole Shelley
- Colhoun Helen
- Colhoun Helen M
- Collins Francis S
- Collins Rory
- Connell John M
- Cooper Cyrus
- Cooper Jackie A
- Cooper Matthew N
- Cooper Richard S
- Coresh Josef
- Cornelis Marilyn C
- Corre Tanguy
- Corsi Anna Maria
- Couper David
- Cousminer Diana L
- Coviello Andrea D
- Cox David
- Crawford Dana
- Crisponi Laura
- Croteau-Chonka Damien C
- Cucca Francesco
- Cummings Steven R
- Cupples Adrienne L
- Cupples L Adrienne
- Curhan Gary
- d'Adamo Pio
- Dahgam Santosh
- Dailiana Zoe
- Danesh John
- Danoy Patrick
- Dastani Zari
- Davies Gail
- Daw E Warwick
- Day Felix R
- Day Ian N M
- de Andrade Mariza
- de Boer Ian H
- de Boer Rudolf A
- de Faire Ulf
- de Geus Eco J C
- Deary Ian J
- Dedoussis George
- Dedoussis George V
- Dedoussis George V Z
- Deelen Joris
- Deelman Ewa
- Dehghan Abbas
- Delgado Graciela
- Deloukas Panagiotis
- Deloukas Panos
- Demerath Ellen W
- Demirkan Ayse
- Demirkan Ayşe
- Den Hertog Heleen M
- Denniff Matthew
- Dennison Elaine M
- Dermitzakis Emmanouil T
- Deshmukh Harshal
- Deshmukh Harshal A
- Devuyst Olivier
- di Meglio Paola
- Diemert Patrick
- Dimas Antigone S
- Dimitriou Maria
- Ding Jingzhong
- Do Ron
- Dominiczak Anna F
- Doney Alex
- Dong Yanbin
- Donnelly Louise A
- Doumatey Ayo
- Dreisbach Albert W
- Drong Alexander W
- Duggan David
- Dumitrescu Logan
- Duncan Bruce B
- Duncan Emma L
- Dupuis Josee
- Dupuis Josée
- Durbin Richard
- Durda Peter
- Döring Angela
- Dörr Marcus
- Eastell Richard
- Easton Douglas F
- Ebrahim Shah
- Econs Michael J
- Edkins Sarah
- Egan Josephine
- Ehret Georg
- Eiriksdottir Gudny
- Eisman John A
- Eklund Niina
- El Mokhtari NourEddine
- Elks Cathy E
- Ellinghaus David
- Elliott Paul
- Elosua Roberto
- Emilsson Valur
- Endlich Karlhans
- Epstein Stephen E
- Erbel Raimund
- Erdmann Jeanette
- Erdos Michael R
- Eriksson Joel
- Eriksson Johan
- Eriksson Niclas
- Eriksson Per
- Ernst Florian
- Esko Tonu
- Esko Tõnu
- Esko Tönu
- Estrada Karol
- Eury Elodie
- Evangelou Evangelos
- Evans Alun
- Evans David M
- Eyheramendy Susana
- Eyjolfsson Gudmundur Ingi
- Fagerholm Emma
- Falhammar Henrik
- Fall Tove
- Farrall Martin
- Fauser Bart C J M
- Fava Cristiano
- Feenstra Bjarke
- Fehrmann Rudolf
- Feitosa Mary
- Feranil Alan B
- Ferrannini Ele
- Ferrario Marco M
- Ferreira Teresa
- Ferreli Liana
- Ferrières Jean
- Ferrucci Luigi
- Fischer Krista
- Florez Jose C
- Folkersen Lasse
- Folsom Aaron R
- Fontanillas Pierre
- Ford Ian
- Fornage Myriam
- Foroud Tatiana
- Forouhi Nita G
- Forrester Terrence
- Forsblom Carol
- Foster Meredith C
- Fowke Jay
- Fowkes F Gerald R
- Fowkes Gerard R
- Fox Caroline S
- Fox Ervin R
- Franceschini Nora
- Franco Oscar H
- Franco-Cereceda Anders
- Franke Andre
- Franke Lude
- Franks Paul W
- Frants Rune
- Fraser Ross M
- Frayling Timothy M
- Freedman Barry I
- Freimer Nelson B
- Freitag Daniel F
- Friedrich Nele
- Froguel Philippe
- Frost Morten
- Fuchsberger Christian
- Galan Pilar
- Ganesh Santhi K
- Ganna Andrea
- Gansevoort Ron T
- Gao Xiaoyi
- Garcia Melissa
- Garcia-Giralt Natàlia
- Garnaas Maija
- Gasparini Paolo
- Gauguier Dominique
- Gaunt Tom R
- Gautvik Kaare M
- Geller Frank
- Gharavi Ali G
- Giedraitis Vilmantas
- Gieger Christian
- Gierman Hinco J
- Gigante Bruna
- Gill Geoffrey V
- Giroux Sylvie
- Giulianini Franco
- Glass Daniel
- Glazer Nicole
- Glazer Nicole L
- Glenn Kim
- Glorioso Nicola
- Go Alan S
- Go Min Jin
- Godson Catherine
- Goel Anuj
- Goessling Wolfram
- Golay Alain
- Goldstein Benjamin A
- Goltzman David
- Gong Jian
- González-Macías Jesús
- Goodall Alison H
- Goodarzi Mark O
- Goodloe Robert
- Gordin Daniel
- Gordon Scott D
- Gorski Mathias
- Grabe Hans-Jörgen
- Graff Misa
- Grallert Harald
- Grammer Tanja B
- Gravito Martha L
- Greenwood Celia M T
- Grewal Jagvir
- Grimsby Jonna
- Grobbee Diederick E
- Groop Leif
- Groop Per-Henrik
- Gross Myron
- Groves Christopher J
- Grundberg Elin
- Grässler Jürgen
- Gräßler Jürgen
- Gu Harvest F
- Gu Tianwei
- Guarrera Simonetta
- Gudbjartsson Daniel F
- Gudnason Villi
- Gudnason Vilmundur
- Guiducci Candace
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- Gyllensten Ulf B
- Hadjadj Samy
- Hadley David
- Haessler Jeff
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- Hall Alistair S
- Hall Per
- Hallan Stein
- Haller Toomas
- Hallmans Goran
- Hallmans Göran
- Hamsten Anders
- Han Bok-Ghee
- Hankinson Susan E
- Hanson Robert L
- Hardy Rebecca
- Haritunians Talin
- Harjutsalo Valma
- Harris Tamara
- Hartikainen Anna-Liisa
- Hartman Catharina A
- Hass Merli
- Hassanali Neelam
- Hassinen Maija
- Hastie Nicholas D
- Hastie Nick
- Hattersley Andrew T
- Haun Margot
- Havulinna Aki S
- Hayward Caroline
- Hazen Stanley L
- He Bing
- He Chunyan
- Heard-Costa Nancy L
- Heath Andrew C
- Heath Simon
- Heckbert Susan R
- Hedblad Bo
- Hedman Åsa K
- Heid Iris M
- Heikkilä Kauko
- Heikkilä Outi
- Heiss Gerardo
- Heliövaara Markku
- Helmer Catherine
- Helmer Quinta
- Henders Anjali K
- Henderson Brian
- Hengstenberg Christian
- Henneman Peter
- Hercberg Serge
- Herder Christian
- Hernandez Dena
- Hernandez Dena G
- Herrera Lizbeth
- Herzig Karl-Heinz
- Hicks Andrew A
- Hietala Kustaa
- Higashio Julia
- Hillege Hans L
- Hilton Gina
- Hindorff Lucia
- Hingorani Aroon
- Hirschhorn Joel N
- Hivert Marie-France
- Ho Weang K
- Hocking Lynne J
- Hoffmann Wolfgang
- Hofman Albert
- Holliday Elizabeth G
- Holm Hilma
- Holmen Oddgeir
- Homuth Georg
- Hopewell Jemma C
- Horikoshi Momoko
- Hosseini Mohsen
- Hottenga Jouke-Jan
- Hovingh G Kees
- Howard Philip
- Hsiung Chao Agnes
- Hsu Yi-Hsiang
- Hu Frank B
- Huang Huateng
- Huang Jinyan
- Hui Jennie
- Humphries Steve E
- Hundertmark Claudia
- Hung Yi-Jen
- Hunt Sarah E
- Hunt Steven C
- Hunter David J
- Husted Lise Bjerre
- Hveem Kristian
- Hwang Shih-Jen
- Hyppönen Elina
- Igl Wilmar
- Ikram M Arfan
- Illig Thomas
- Imboden Medea
- Ingelsson Erik
- Ingle Catherine
- Ingvarsson Thorvaldur
- Ioannidis John P A
- Iribarren Carlos
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- Isakova Tamara
- Islam Muhammad
- Ittermann Till
- Iwai Naoharu
- Jackson Anne U
- Jackson Rebecca
- Jacobs Gunnar
- Jafar Tazeen H
- James Alan L
- Jameson Karen A
- Jang Yangsoo
- Janipalli Charles S
- Jansen Hanneke
- Janssens A Cecile J W
- Jarvelin Marjo-Riitta
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- Johansen Berit
- Johansson Ingegerd
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- Johnson Andrew
- Johnson Louise
- Johnson Paul C D
- Johnson Toby
- Jones Graeme
- Jones Michelle R
- Jousilahti Pekka
- Ju Sung Yun
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- Kammerer Candace M
- Kanaya Alka
- Kang Hyun M
- Kang Hyun Min
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- Kaptoge Stephen K
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- Kardia Sharon L
- Karjalainen Juha
- Karlsson Magnus
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- Kastelein John J P
- Kathiresan Sekar
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- Kedenko Lyudmyla
- Kee Frank
- Keildson Sarah
- Keinanen-Kiukaanniemi Sirkka M
- Keller Benjamin J
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- Kessler Thorsten
- Kestenbaum Bryan
- Kesäniemi Antero
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- Kettunen Johannes
- Keyzer Jules
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- Khusnutdinova Elza
- Kiel Douglas P
- Kiess Wieland
- Kilpeläinen Tuomas O
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- Kita Yoshikuni
- Kivimaki Mika
- Kizer Jorge R
- Klaric Irena Martinovic
- Kleber Marcus E
- Klopp Norman
- Kloppenburg Margreet
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- Knowles Joshua W
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- Koenig Wolfgang
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- van Wingerden Sophie
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- Van Zuydam Natalie
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- Verlaan Dominique
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- Wagenknecht Lynne E
- Waggott Daryl
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- Wallaschofski Henri
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- Wang Jie Jin
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- Wichmann H Erich
- Wichmann H-Erich
- Widen Elisabeth
- Wiggins Kerri L
- Wijmenga Cisca
- Wijnands-van Gent Colette J M
- Wild Philipp S
- Wild Sarah H
- Wilk Alicja
- Wilkens Lynne
- Willems Sara M
- Willemsen Gonneke
- Willemsvan-vanDijk Ko
- Willenborg Christina
- Willer Cristen J
- Williams Frances M K
- Williams Rasheeda
- Williams Winfred W
- Willner Dana
- Wilsgaard Tom
- Wilson James F
- Wilson James G
- Wilson Sarah
- Wilson Scott G
- Winkler Thomas
- Witteman Jacqueline C
- Witteman Jacqueline C M
- Wojczynski Mary K
- Wolffenbuttel Bruce H R
- Wong Andrew
- Wong Tien Y
- Woo Jean
- Wood Andrew R
- Wood Andy
- Workalemahu Tsegaselassie
- Wright Alan F
- Wu Chunyuan
- Wu Joseph M W
- Wu Ying
- Würtz Peter
- Xiao Su-Mei
- Yajnik Chittaranjan S
- Yang Jian
- Yang Qiong
- Yang Tsun-Po
- Yao Jie
- Yengo Loïc
- Yerges-Armstrong Laura M
- Young Alicia
- Young Elizabeth H
- Young J H
- Young Lauren
- Yuan Xin
- Zaboli Ghazal
- Zalloua Pierre A
- Zarrabeitia María T
- Zelenika Diana
- Zemunik Tatijana
- Zerbini Gianpaolo
- Zgaga Lina
- Zhai Guangju
- Zhang Feng
- Zhang Qunyuan
- Zhang Weihua
- Zhao Jing Hua
- Zhao Wei
- Zheng Hou-Feng
- Zheng Wei
- Zhou Yanhua
- Zhu Haidong
- Zhu Kun
- Zhu Xiaofeng
- Zhuang Wei V
- Zhuang Wei Vivian
- Ziegler Andreas
- Zillikens M Carola
- Zimmermann Martina E
- Zitting Paavo
- Zondervan Krina T
- Zukowska-Szczechowska Ewa
- Zygmunt Marek
- Ärnlöv Johan
- Österholm Anne-May
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our understanding of the genetic basis of body fat distribution and its molecular links to cardiometabolic traits, here we conduct genome-wide association meta-analyses of traits related to waist and hip circumferences in up to 224,459 individuals. We identify 49 loci (33 new) associated with waist-to-hip ratio adjusted for body mass index (BMI), and an additional 19 loci newly associated with related waist and hip circumference measures (P < 5 × 10(-8)). In total, 20 of the 49 waist-to-hip ratio adjusted for BMI loci show significant sexual dimorphism, 19 of which display a stronger effect in women. The identified loci were enriched for genes expressed in adipose tissue and for putative regulatory elements in adipocytes. Pathway analyses implicated adipogenesis, angiogenesis, transcriptional regulation and insulin resistance as processes affecting fat distribution, providing insight into potential pathophysiological mechanisms
Finishing the euchromatic sequence of the human genome
- Author
- . Haifeng
- . Magner
- . Yin
- Abbott Scott
- Abbott-Ozersky Amanda
- Abdellah Zahra
- Abouelleil Amr
- Abrajano Anne
- Adachi Tamami
- Adam Catherine
- Adams Charles Q.
- Adamson Aaron
- Adekoya Emmanuel
- Adio-Oduola Babajide
- Aerts Andrea
- Aggarwal Arun
- Ahmadi Alireza
- Ahmed Shahana
- Aimable Matthew
- Ainscough Rachael
- Ait-Zahra Mostafa
- Aizu Tomoyuki
- Alcivare Dana
- Alegria Michelle
- Ali Alla
- Ali Johar
- Allegria-hartmann Michelle
- Alleman Jennifer
- Allen Carlana C.
- Allen Heather
- Allen Nicole R.
- Allen Susan
- Allen Thaddeus
- Almeida Jeff
- Almond Claire
- Alsbrooks Stephen L.
- Altherr Michael R.
- Amaratunge Harshinie C.
- Ambler Andrew
- Ambrose Karen
- Ambrose Kerrie
- Amemiya Chris
- Amico-Keller Gina
- Amin Amita G.
- Anderson Mechele
- Anderson Scott
- Anderson Scott
- Andora Janice
- Andredesz Carol
- Andrew Robert
- Andrews Dan
- Andrews Daniel
- Andrews Neil
- Andrews Stephanie
- Andriese Tim
- Anthouard Véronique
- Antonarakis Stylianos E.
- Anyalebechi Vivian
- Aoki Norie
- Apostolou Sinoula
- Apweiler Eva
- Arachchi Harindra
- Arai Rie
- Arbery Hazel
- Arcaina Marlon
- Arcaina Terisita
- Archer Beth
- Arellano Andre
- Arellano-Jones Perry
- Armbruster Jeff
- Armstrong Jon
- Arredondo Dilrukshi P.
- Arredondo Heather Hope
- Artiguenave François
- Asakawa Shuichi
- Asakawa Teruyo
- Ash Gareth
- Ashcroft Kevin
- Ashurst Jennifer
- Ashwell Robert
- Ashworth Linda K.
- Aslanidis Cara
- Asomugha Chinwe O.
- Asuncion Lawreen
- Atkin Deborah
- Atkinson Andrea
- Atkinson Barry
- Attix Cristina
- Attwood John
- Aubin Keith
- Auger Katherine
- Austin Shannon Michelle
- Avila Aaron
- Avis Terry
- Ayele Mulu
- Babayan Primo
- Babbage Anne
- Babbage Sarah
- Bach Phil
- Bachatsang Pasang
- Bacon Joanne
- Badri Hummy
- Baertsch Robert
- Bagguley Claire
- Bailey Jonathan
- Bajorek Eva
- Baker Andrew
- Baker Dan
- Baker M.
- Baker Richard
- Bakis Michele
- Baldwin Jennifer
- Banda Michael
- Banerjee Ruby
- Bao Jingyue
- Bao Qiyu
- Bao Weidong
- Bao Weidong
- Baptiste Pertrice
- Barbaria Joseph A.
- Barbe Valérie
- Bardill Simon
- Barker Daniel
- Barker Darren
- Barker Gary
- Barlow Karen
- Baron Laurent
- Barrett Anika
- Bartlett Rebecca
- Basham Victoria
- Bashman David
- Basu Suba
- Bateman Alex
- Bates Karen
- Battles John
- Batzer Mark
- Baumgart Cornelia
- Baumohl Jason
- Baynes Caroline
- Bayul Tashi
- Beall Keith
- Beard Lisa
- Beard Susan
- Beare David
- Beasley Alastair
- Beasley Helen
- Beasley Oliver
- Beaucham Leslie
- Beaudet Arthur
- Beck Alfred
- Beck Stephen
- Becker Michael
- Bell Emma
- Bell George I.
- Bellard Terell M.
- Bellerby Damian
- Bellerby Tristram
- Belter Edward A., Jr.
- Bemrose Richard
- Benard Michael Anthony
- BenKahla Alia
- Benke J
- Benner William
- Bennett James
- Bensasson Douda
- Bentley Andrew
- Bentley Dan
- Bentley David
- Berardinis Véronique de
- Bercovitz John
- Berghoff Amy
- Bergmann Anne
- Berkowicz Nicolas
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- Beugelsdijk Tony J.
- Bhakta Rita
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- Bimage Kesha E.
- Bird Christine
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- Blomstrom David B.
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- Bloom Toby
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- Blye Jason
- Blyth Peter R.
- Blöcker Helmut
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- Brandriff Brigitte F.
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- Hitchens Matthew Edward
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- Krawczyk Marie-Claude
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- Kremmidiotis Gabriel
- Krogh Anders
- Kronmiller Brent
- Kruchowski Scott S.
- Kube Michael
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- Loveland Jane
- Lovell Jamie
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- Lowry Stephen
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- Lu Lingfeng
- Lu Tao
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- Lu Yue
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- Lucas Susan
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- Lucier Raymond L.
- Ludeman Thom
- Lui Annie
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- Macdonald Pendexter
- Machrus Migdad
- Macht Madison
- Macken Catherine A.
- MacLean Christine
- Madabhushi Ramki
- Madu Renita C.
- Maeda Hideto
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- Maheshwari Manjula
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- Maltbie Mary I.
- Mangum Brian
- Manning Jonathan
- Manohar Chitra
- Mapua Patricia
- Marabella Dick
- Mardis Elaine R.
- Mareth David
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- Marinelli Lisa
- Mark Graham A.
- Marquis-Homeyer Catherine
- Marr Thomas G.
- Marra Marco
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- Wu Zaining
- Wyatt Julia
- Wycoff-Montenegro Melissa
- Wylie Kris
- Wyman Dudley
- Wyman Stacia
- Xi Yan
- Xi Yingying
- Xie Fei
- Xie Gary
- Xie Jane
- Xiong Hui
- Xiong Yuqing
- Xu Alex
- Xu Jing
- Xu Jing
- Xu Ruqin
- Xu Shuhua
- Xu Wei
- Xu Xinlai
- Xu Yan
- Xu Yuning
- Xu Zhihong
- Xu Zuyuan
- Xuan Yali
- Xuan Zhenyu
- Xue Rui
- Yada Tetsushi
- Yadav Shailendra
- Yakub Syed
- Yamamoto Lynn
- Yamamoto Noriko
- Yamamoto Yuko
- Yamashita Yasue
- Yamazaki Satoru
- Yang Hao
- Yang Huanming
- Yang Huanming
- Yang Joan
- Yang Shiaw-Pyng
- Yang Shudong
- Yang Xiaonan
- Yang Xiaonan
- Yang Xiaoping
- Yang Yongkui
- Yano Candance
- Yao Zhijian
- Yao Zhijian
- Yaspo Marie-Laure
- Ye Chen
- Yeager Shane
- Yeh Mimi
- Yen Jennifer
- Yeshitela Rahel Retta
- Yoakum Martin
- Yokobata Kathy
- Yokoyama Jennifer
- Yonezawa Miho
- Yoon Lillienne
- Yoon Vivienne
- Yoshida Satoru
- You Bo
- Young Geneva
- Young Louise
- Young Shelia
- Younger Ruth
- Yu Bing
- Yu Charles
- Yu Fuli
- Yu Jun
- Yu Jun
- Yu Jun
- Yuan Kaiwen
- Yuan Ye
- Yuan Yida
- Yue Shujie
- Yumae Brian
- Yun Rui
- Zainoun Joanne
- Zembeck Lisa
- Zeng Yixin
- Zhai Dong
- Zhan Guoping
- Zhang Bo
- Zhang Caimin
- Zhang Fengmei
- Zhang Guangyu
- Zhang Guohua
- Zhang Guohua
- Zhang Haiqing
- Zhang Haiqing
- Zhang Haiqing
- Zhang Hongbo
- Zhang Hongbo
- Zhang Jingjing
- Zhang Jingjing
- Zhang Jingkun
- Zhang Jiuchun
- Zhang Jiuchun
- Zhang Lanzhi
- Zhang Li
- Zhang Li
- Zhang Meihua
- Zhang Meng
- Zhang Ming
- Zhang Qing
- Zhang Ruhua
- Zhang Shaojie
- Zhang Tiezhen
- Zhang Wei
- Zhang Wei
- Zhang Xianglin
- Zhang Xianglin
- Zhang Xiaoliang
- Zhang Xiuqing
- Zhang Yan
- Zhang Yi
- Zhang Yilin
- Zhang Yilin
- Zhang Ying
- Zhang Yuansen
- Zhang Yuzhi
- Zhang Zhengdong
- Zhao Hongmei
- Zhao Lijian
- Zhao Shenru
- Zhao Zhijing
- Zhen Zhicheng
- Zheng Haibo
- Zhong Ming
- Zhou Carol
- Zhou Haixia
- Zhou Jianling
- Zhou Nannan
- Zhou Xinfeng
- Zhou Yan
- Zhou Yang
- Zhou Yi
- Zhu Bingying
- Zhu Bofeng
- Zhu Fenghua
- Zhu Genfeng
- Zhu Genfeng
- Zhu Miao
- Zhu Ning
- Zhu Yongge
- Zhu Zhen
- Zhuang Shitao
- Zierten Deborah
- Zimmer Andrew
- Zody Michael C.
- Zollo Massimo
- Zorrilla Sara E.
- Zuo Lin
- Publication venue
- LSU Digital Commons
- Publication date
- 21/10/2004
- Field of study
The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead
25th annual computational neuroscience meeting: CNS-2016
- Author
- Abbott L.F.
- Abeysuriya Romesh G.
- Aertsen Ad
- Agnes Everton J.
- Ahamed Tosif
- Ahmadabadi Majid Nili
- Ahn Sora
- Aihara Kazuyuki
- Aihara Kazuyuki
- Andreassen Ole A.
- Andreassen Ole A.
- Ardestani Mohammad Hovaidi
- Ardestani Mohammad Hovaidi
- Arroyo David
- Aton Sara J.
- Babichev Andrey
- Bachmann Claudia
- Badel Laurent
- Baek Hyeon-Man
- Baek JeongHun
- Baek Kwangyeol
- Bahuguna Jyotika
- Bak Ji Hyun
- Baker Chris I.
- Bakker Rembrandt
- Balaguer‑Ballester Emili
- Bard G.
- Barnett William H.
- Baroni Fabiano
- Basnayake Kanishka
- Baysal Velt
- Bennett Matthew R.
- Bernard Christophe
- Berry Hugues
- Beuth Frederick
- Bezgin` Gleb
- Bill Johannes
- Birgolias Justas
- Blackwell Justin
- Bohnenkamp Lisa
- Bojak Ingo
- Borisyuk Roman
- Bos Hannah
- Bradley Samual P.
- Breakspear Michael
- Breitwieser Oliver
- Briaire` Jeroen J.
- Briggman Kevin L
- Brinkman Braden A.
- Brown John
- Brown Ritchie E.
- Brunel Nicolas
- Buhry Laure
- Buice Michael
- Burkitt Anthony N.
- Burton Shawn D.
- Buttler Simone
- Bytschok Ilja
- Cantarelli Matteo
- Chakravarthy V.Srinivasa
- Chan Ho Ka
- Chapman Phillip D.
- Chatzikalymniou Alexandra Pierri
- Chavane Frédéric
- Chen Liang
- Chen Weiliang
- Cheung Chung Ching
- Chhabria Karishma
- Chintaluri Chaitanya
- Choe Yoonsuck
- Choi Hannah
- Choi Hansol
- Choi Ilhwan
- Choi Jee Hyun
- Choi Woochul
- Choi Yun Seo
- Choung Oh‑hyeon
- Chung SueYeon
- Clarke Eric F.
- Clements Katie
- Cloherty Shaun L.
- Clopath Claudia
- Cocchi Luca
- Cohen Yale E.
- Cook Mark
- Crook Sharon M.
- Cserpán Dorottya
- Culmone Viviana
- Dabaghian Yuri
- Dabaghian Yuri
- Dale Anders M.
- Daly Kevin C.
- Dasgupta Sakyasingha
- Davey Neil
- Davey Neil
- Davison Andrew
- de Weerd Peter
- Deco Gustavo
- Demkó László
- Demutz Harald
- Denk Cornelia
- Destexhe Alain
- Devor Anna
- DeVuti Justin
- Diamond Alan
- Diesmann Markus
- Dillen Kim
- Doya Kenji
- Dragoi Valentin
- Draguljić Daniel
- Drew Jordan
- Drysdale Peter M.
- Duarte Renato
- Dura‑Bernal Salvador
- Dura‑Bernal Salvador
- Dura‑Bernal Salvador
- Edwards Andy
- Einevoll Gaute T.
- Elices Irene
- Elnevoll Gaute T.
- Ernst Udo A.
- Esler Timothy B.
- Esposito Elric
- Faraji Mohammad Java
- Fedorov Leonid A.
- Fenk Lisa M.
- Ferguson Katie
- Ferrario Andrea
- Filipovi Marko
- Fink Christian G.
- Fink Gereon R.
- Fishman Yonatan I.
- Fornito Alex
- Forrow Csaba
- Fouquet Coralie
- Frangou Sophia
- Freestone Dean R.
- Frijns Johan H. M.
- Fulcher Ben D.
- Fung Felix
- Gajic N. Alex Cayco
- Gallimore Andrew R.
- Gallinaro Júlia
- Gerkin Richard C.
- Gerstner Wulfram
- Giaffar Hamza
- Giese Martin
- Giese Martin
- Giese Martin A.
- Gilson Matthieu
- Gips Bart
- Gleeson Padraig
- Gliske Stephen V.
- Glomb Katharina
- Goetze Felix
- Goldsworthy Mitchell R.
- Gollo Leonardo L.
- Goncharenko Julia
- Goodarzinic Abdorreza
- Graham Bruce P.
- Grayden David B.
- Grayden David B.
- Grewe Jan
- Hadrava Michal
- Hagen Espen
- Halnes Geir
- Halnes Geir
- Hamade Khaldoun
- Hamker Fred H.
- Han Hio-Been
- Han Seung Kee
- Hansen Mads
- Harper Zachary J.
- He Hu
- Helias Moritz
- Hermann Christoph S.
- Hilgetag` Claus‑Christian
- Hines Michael L.
- Hlinka Jaroslav
- Hof Patrick R.
- Holman Katherine A.
- Hong Sungho
- Hordacre Brenton
- Howard Jr. James H.
- Huang Guang-Bin
- Huang Haiping
- Huerta Ramon
- Huh Dongsung
- Hutt Axel
- Hwang Dong‑Uk
- Hwang Eunjin
- Hye Jr. Eoon
- Iannella Nicolangelo
- Iannella Nicolangelo
- Ibbotson Michael R.
- Ionta Silvlo
- Ishii Shin
- Issa Fadi A.
- Iyer Ramakrishnan
- Jacobs Heidi
- Jang Hyun Jae
- Jang Jaeson
- Jang Jaeson
- Jensen Ole
- Jeong Jaeseung
- Jeong Jaesung
- Jeong Yong
- Jirsa Viktor K.
- Jo Sumin
- Joo Pangyu
- Josić Kresimir
- Ju Huiwen
- Jun Eunji
- Jun Sang Beom
- Jung Nam
- Jung Woo-Sung
- Jung Younginha
- Kahng B.
- Kale Penelope J.
- Kalkman Randy K.
- Kameneva Tatiana
- Kameneva Tatiana
- Kang Jiyoung
- Karoly Philippa J.
- Kasumi Ohta
- Kavalali Enge T.
- Kawato Mitsuo
- Kazama Hokto
- Kedziora David J.
- Kekona Tyler
- Keller Daniel
- Kennedy Henry
- Kepple Daniel
- Kerr Cliff C.
- Kerr Robert R.
- Kilpatrick Zachary P.
- Kim Ammo J.
- Kim Bowon
- Kim Bowon
- Kim Chang Sub
- Kim DaeEun
- Kim Hojeong
- Kim Hoon-Hee
- Kim Hyoungkyu
- Kim Jae Kyoung
- Kim Jimin
- Kim Jinseop
- Kim Juhee
- Kim Minjung
- Kim Seongkyun
- Kim Su Hyun
- Kim Sung-Phil
- Kim Sung-Phil
- Kim Tae
- Kim Taegyo
- Kim Won Sup
- Kim Youngsoo
- Kiser Seth A.
- Klanner Felix
- Kleberg Florence I.
- Klingbeil Guido
- Knösche Thomas
- Koren Veronika
- Koren Veronika
- Kotaleski Jeanette Hellgren
- Koulakov Alex
- Kralik Jerald D.
- Kringelbach Morten L.
- Kruscha Alexandra
- Kuhlmann Levin
- Kukolja Juraj
- Kumar Arvind
- Kumar Arvind
- Kundu Prantik
- Kunze Tim
- Kuravi Pradeep
- Kwag Jeehyun
- Kwon Jaehyung
- Lai Pik‑Yin
- Lakatos Peter
- Latorre Roberto
- Leahy Will
- Lee Changju
- Lee Chungho
- Lee Dan D.
- Lee Do-won
- Lee Heonsoo
- Lee Hyang Jung
- Lee Hyang Woon
- Lee Hyeonsu
- Lee Jae Woo
- Lee Jaejin
- Lee Jeungmin
- Lee Joonwon
- Lee Jung H.
- Lee Sang Wan
- Lee Sang-Hun
- Lee Seungjun
- Lee Soohyun
- Lee Sue-Hyun
- Lee Tae Ho
- Lee Won Hee
- Lee Yong‑il
- Lefebvre Baptiste
- Lefebvre Jérémie
- Leleu Timothée
- Leng Luziwei
- Levi Rafael
- Levina Anna
- Levy Brandon A.
- Li Luozheng
- Liang Guangsheng
- Lidner Benjamin
- Liedtke Joscha
- Lim Daeseob
- Lim Sewoong
- Lin Xiahoan
- Linder Benjamin
- Lines Glenn T.
- Lizler Joseph T.
- Lochmann Timm
- Lowet Eric
- Luebke Jennifer
- Lytton William W.
- Lytton William W.
- Lyu Cheng
- Ma Hailin
- Maeng Seung Eu
- Malmon Gabby
- Mandall Alekhya
- Maouene M.
- Marcelli Angelo
- Marin Boris
- Markin Sergey
- Markram Henry
- Marre Olivier
- Marsalek Petr
- Marsat Gary
- Martel Roman
- Marucci Lucia
- Maturana Matias I.
- McCarley Robert W.
- McDonnell Mark D.
- McDonnell Mark D.
- McKenna James T.
- McLauchlan Campbell
- Meffin Hamish
- Meffin Hamish
- Mehta Hima
- Meier Karlheinz
- Meijas Jorge F.
- Mellen Nick
- Memmeshei Raol-Martin
- Menzies Rosemary J.
- Merriosn-Hort Robert
- Metzner Christoph
- Mi Yuanyuan
- Mi Yuanyuan
- Mihalas Stefan
- Miller Thomas
- Moezzi Bahar
- Moezzi Bahar
- Molkov Yaroslav I.
- Moon Jangsup
- Moon Seok-hun
- Morris Laurel S.
- Morrison Abigail
- Mosqueiro Thiago S
- Mu Shang
- Muler Eilif
- Muralidharan Vignesh
- Murray John D.
- Murray Micha M.
- Mäki‑Marttunen Tuomo
- Neymotin Samuel
- Neymotin Samuel A.
- Niry Mohammad
- Nishikawa Isao
- Nolte Max
- Nowotny Thomas
- Oba Shigeyuki
- Obermayer Klaus
- Obermayer Klaus
- Ognjanovski Nicolette
- Ouyang Guang
- Ozer Mahmut
- Paik Se-Bum
- Paik Se‑Bum
- Palmer S.E.
- Palva Matias J.
- Paninski Liam
- Pariz Aref
- Park Chang-hyun
- Park Choongseok
- Park Hae‑Jeong
- Park Ji Sung
- Park Memming
- Park Sang-Min
- Park Sol
- Parsi Shervin S.
- Parziale Antonio
- Pasupathy Anitha
- Perotti Luca
- Peterson Andre
- Petkoski Spase
- Petrovici Mihai A.
- Petterson Klas H.
- Philips Ryan T.
- Phillips Ryan S.
- Pillow Jonathan
- Pittà Maurizio De
- Plogmacher Lukas
- Podlaski William
- Pollonini Luca
- Ponce‑Alvarez Adrián
- Popp Pamela Osborn
- Preuschoff Kerstin
- Priesemann Viola
- Priesemann Viola
- Priyadharsini B. Praga
- Psarrou Maria
- Quang Le Anh
- Quintana Adrian
- Ramsey Julia
- Ranjan Rajnish
- Rankin James
- Rankin James
- Rasch Malte J.
- Rasuli Nader
- Ratnadurai‑Giridharan Shivakeshavan
- Reig Ramon
- Reimann Michael W.
- Rennle Chris J.
- Reyes Amy
- Richter René
- Ridding Michael C.
- Rieke Fred
- Rinberg Dima
- Rinzel John
- Ritter Petra
- Roach James P.
- Robb Daniel T.
- Roberts Mark J.
- Robinson Peter A.
- Robinson Peter A.
- Rodriguez Francisco B.
- Rotter Stefan
- Rubchinsky Leonid L.
- Rubinov Mikail
- Rumbell Timothy
- Rupp André
- Rybak Ilya A.
- Ryu Juhyoung
- Sadeh Sadra
- Saggio Maria L.
- Sander Leonard M.
- Sanger Terence D.
- Sanz-Leon Paula
- Sanz‑Leon Paula
- Saska Daniel
- Schaworonkow Natalie
- Schemmel Johannes
- Scheutz Matthias
- Schiff Steven J.
- Schilstra Maria
- Schilstra Marla
- Schmidt Maximilian
- Schmidt Robert
- Schottdorf Manual
- Schutter Erik De
- Schwikard Achim
- Seeholzer Alexander
- Seidenstein Alexandra
- Sejnowski Terrence J.
- Sekulić Vladisla
- Senatore Rosa
- Senk Johanna
- Seo Sat Byul
- Seung H. Sebastian
- Sharpee Tatyana O.
- Shea Steven
- Shea-Brown Eric
- Shea‑Brown Eric
- Shen Kelly
- Shiau LieJune
- Shimazaki Hideaki
- Shin Hee‑sup
- Shin In-Seob
- Shivkumar Sabyasach
- Shlizerman Eli
- Shomali Safura Rashid
- Siep Silvan F.
- Silberberg Gilad
- Silver Angus
- Silver R. Angus
- Skiker K.
- Skilling Quinton M.
- Skinner Frances K.
- Skinner Frances K.
- Smit Daniel
- Smith Brian
- Smith Jeffrey
- Soh Jaehyun
- Soman Karthik
- Somogyvári Zoltán
- Sompolinsky Haim
- Song Min
- Song Min-Ho
- Song Youngjo
- Soundry Daniel
- Sourina Olga
- Spampinato Giulia Lia Beatrice
- Spiegler Andreas
- Spinney Richard E.
- Sprecher Simon
- Stacey William C.
- Stacey William C.
- Stephens Greg
- Stern Merav
- Steuber Volker
- Steyn-Ross D. Alistair
- Steyn-Ross Moira L.
- Stimberg Marcel
- Strube‑Bloss Martin F.
- Stöckel David
- Su Jianzhong
- Sun Haoqi
- Sweeney Yann
- Tabas Alejandro
- Tahayori Bahman
- Takashima Akira
- Tam Nicoladie D.
- Tamagnini Francesco
- Tang Rongxiang
- Tang Yi-Yuan
- Tang Yi-Yuan
- Teka Wondimu
- Tetzlaff Tom
- Tezuka Taro
- Toporikova Natalia
- Torres Joaquin J.
- Toyoizumi Taro
- Tran Patricia H. P.
- Trembleau Alain
- Triesch Jochen
- Trisch Jochen
- Tsaneva‑Atanasova Krasimira
- Tsuchimoto Yoshiko
- Tuomo Maki-Martun
- Tveito Aslak
- Valizadeh Alireza
- Valizadeh Alireza
- van Albada Sacha J
- van Albada Sacha J.
- van der Eerden Jan
- Varona Pablo
- Varona Pablo
- Veale Richard
- Viriyopase Atthaphon
- Vitay Julien
- Vogels Rufin
- Vogels Tim
- Vogels Tim P.
- Vogt Simon M.
- Voon Valerie
- Voronenko Sergej O.
- Vuust Peter
- Vörös János
- Wallentin Mikkel
- Wang Dahui
- Wang Jisung
- Wang Sheng-Ju
- Wang Yuzhe
- Warburton Julia M.
- Weaver Christina M.
- Wegener Detlef
- Weidel Philipp
- Welzig Charles M.
- Werdt Stephen Van
- Wibral Michael
- Wickens Jeffery R.
- Widmer Yves
- Witek Maria A. G.
- Witting Jens
- Wolf Fred
- Wong Michael
- Wu Si
- Wu Sl
- Wójcik Daniel K.
- Xu Zhiheng
- Yamada Yasnori
- Yamamura Yorkio
- Yang Huei-Fang
- Yang Xu
- Yeon Ji Won
- Yger Pierre
- Yilmaz Ergin
- Yoo Minsu
- Yoon Sangsup
- Yoshimoto Junichiro
- Young-Ah Rho
- Yu Suin
- Zaho Yuan
- Zamora Criseida
- Zaptocky Martin
- Zhang Mingsha
- Zhang Wenhao
- Zhao Chang
- Zhao Xiaochen
- Zhao Xuelong
- Zhou Changsong
- Zochowski Michal
- Zochowski Michal R.
- Zouridakis George
- Zurowski Bartosz
- Publication venue
- BMC
- Publication date
- 01/01/2016
- Field of study
The same neuron may play different functional roles in the neural circuits to which it belongs. For example, neurons in the Tritonia pedal ganglia may participate in variable phases of the swim motor rhythms [1]. While such neuronal functional variability is likely to play a major role the delivery of the functionality of neural systems, it is difficult to study it in most nervous systems. We work on the pyloric rhythm network of the crustacean stomatogastric ganglion (STG) [2]. Typically network models of the STG treat neurons of the same functional type as a single model neuron (e.g. PD neurons), assuming the same conductance parameters for these neurons and implying their synchronous firing [3, 4]. However, simultaneous recording of PD neurons shows differences between the timings of spikes of these neurons. This may indicate functional variability of these neurons. Here we modelled separately the two PD neurons of the STG in a multi-neuron model of the pyloric network. Our neuron models comply with known correlations between conductance parameters of ionic currents. Our results reproduce the experimental finding of increasing spike time distance between spikes originating from the two model PD neurons during their synchronised burst phase. The PD neuron with the larger calcium conductance generates its spikes before the other PD neuron. Larger potassium conductance values in the follower neuron imply longer delays between spikes, see Fig. 17.Neuromodulators change the conductance parameters of neurons and maintain the ratios of these parameters [5]. Our results show that such changes may shift the individual contribution of two PD neurons to the PD-phase of the pyloric rhythm altering their functionality within this rhythm. Our work paves the way towards an accessible experimental and computational framework for the analysis of the mechanisms and impact of functional variability of neurons within the neural circuits to which they belong
Recommended from our members
Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021
- Author
- Aali Amirali
- Ababneh Hazim S
- Abate Yohannes Habtegiorgis
- Abbafati Cristiana
- Abbasgholizadeh Rouzbeh
- Abbasi-Kangevari Mohsen
- Abbasian Mohammadreza
- Abbastabar Hedayat
- Abd ElHafeez Samar
- Abd-Elsalam Sherief
- Abdelmasseh Michael
- Abdelwahab Ahmed
- Abdollahi Mohammad
- Abdollahifar Mohammad-Amin
- Abdoun Meriem
- Abdulah Deldar Morad
- Abdullahi Auwal
- Abebe Mesfin
- Abebe Samrawit Shawel
- Abedi Aidin
- Abegaz Kedir Hussein
- Abhilash E S
- Abidi Hassan
- Abiodun Olumide
- Aboagye Richard Gyan
- Abolhassani Hassan
- Abolmaali Meysam
- Abouzid Mohamed
- Aboye Girma Beressa
- Abreu Lucas Guimarães
- Abrha Woldu Aberhe
- Abtahi Dariush
- Abu Rumeileh Samir
- Abu-Gharbieh Eman
- Abu-Rmeileh Niveen ME
- Abu-Zaid Ahmed
- Abualruz Hasan
- Abubakar Bilyaminu
- Aburuz Salahdein
- Accrombessi Manfred Mario Kokou
- Adal Tadele Girum
- Adamu Abdu A
- Addo Isaac Yeboah
- Addolorato Giovanni
- Adebiyi Akindele Olupelumi
- Adekanmbi Victor
- Adepoju Abiola Victor
- Adetunji Charles Oluwaseun
- Adetunji Juliana Bunmi
- Adeyeoluwa Temitayo Esther
- Adeyinka Daniel Adedayo
- Adeyomoye Olorunsola Israel
- Admass Biruk Adie Adie
- Adnani Qorinah Estiningtyas Sakilah
- Adra Saryia
- Afolabi Aanuoluwapo Adeyimika
- Afzal Muhammad Sohail
- Afzal Saira
- Agampodi Suneth Buddhika
- Agasthi Pradyumna
- Aggarwal Manik
- Aghamiri Shahin
- Agide Feleke Doyore
- Agodi Antonella
- Agrawal Anurag
- Agyemang-Duah Williams
- Ahinkorah Bright Opoku
- Ahmad Aqeel
- Ahmad Danish
- Ahmad Firdos
- Ahmad Muayyad M
- Ahmad Sajjad
- Ahmad Shahzaib
- Ahmad Tauseef
- Ahmadi Keivan
- Ahmadzade Amir Mahmoud
- Ahmed Ali
- Ahmed Ayman
- Ahmed Haroon
- Ahmed Luai A
- Ahmed Mehrunnisha Sharif
- Ahmed Meqdad Saleh
- Ahmed Muktar Beshir
- Ahmed Syed Anees
- Ajami Marjan
- Aji Budi
- Akara Essona Matatom
- Akbarialiabad Hossein
- Akinosoglou Karolina
- Akinyemiju Tomi
- Akkaif Mohammed Ahmed
- Akyirem Samuel
- Al Hamad Hanadi
- Al Hasan Syed Mahfuz
- Al-Aly Ziyad
- Al-amer Rasmieh Mustafa
- Al-Azzam Sayer
- Al-Gheethi Adel Ali Saeed
- Al-Hanawi Mohammed Khaled
- Al-Marwani Sabah
- Al-Maweri Sadeq Ali Ali
- Al-Mekhlafi Hesham M
- Al-Omari Basem
- Al-Sabah Salman Khalifah
- Al-Tawfiq Jaffar A
- Al-Worafi Yaser Mohammed
- Alahdab Fares
- Alalalmeh Samer O
- Alalwan Tariq A
- Alam Khurshid
- Alam Manjurul
- Alam Noore
- Alanezi Fahad Mashhour
- Alanzi Turki M
- Albakri Almaza
- Albashtawy Mohammed
- AlBataineh Mohammad T
- Alcalde-Rabanal Jacqueline Elizabeth
- Aldawsari Khalifah A
- Aldhaleei Wafa A
- Aldridge Robert W
- Alema Haileselasie Berhane
- Alemayohu Mulubirhan Assefa
- Alemi Sharifullah
- Alemu Yihun Mulugeta
- Alhabib Khalid F
- Alhalaiqa Fadwa Alhalaiqa Naji
- Ali Abid
- Ali Amjad
- Ali Liaqat
- Ali Mohammed Usman
- Ali Rafat
- Ali Shahid
- Ali Syed Shujait Shujait
- Alicandro Gianfranco
- Alif Sheikh Mohammad
- Alikhani Reyhaneh
- Alimohamadi Yousef
- Aliyi Ahmednur Adem
- Aljasir Mohammad A M
- Aljunid Syed Mohamed
- Alla François
- Allebeck Peter
- Almazan Joseph Uy
- Almidani Louay
- Almidani Omar
- Alomari Mahmoud A
- Alonso Jordi
- Alqahtani Jaber S
- Alqalyoobi Shehabaldin
- Alqutaibi Ahmed Yaseen
- Altaany Zaid
- Altaf Awais
- Altirkawi Khalid A
- Aluh Deborah Oyine
- Alvis-Guzman Nelson
- Alwafi Hassan
- Aly Hany
- Aly Safwat
- Alzoubi Karem H
- Amani Reza
- Amare Azmeraw T
- Amegbor Prince M
- Ameyaw Edward Kwabena
- Amin Tarek Tawfik
- Amindarolzarbi Alireza
- Amiri Sohrab
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- Ärnlöv Johan
- Šekerija Mario
- Publication venue
- Elsevier
- Publication date
- 03/04/2024
- Field of study
BACKGROUND Regular, detailed reporting on population health by underlying cause of death is fundamental for public health decision making. Cause-specific estimates of mortality and the subsequent effects on life expectancy worldwide are valuable metrics to gauge progress in reducing mortality rates. These estimates are particularly important following large-scale mortality spikes, such as the COVID-19 pandemic. When systematically analysed, mortality rates and life expectancy allow comparisons of the consequences of causes of death globally and over time, providing a nuanced understanding of the effect of these causes on global populations. METHODS The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 cause-of-death analysis estimated mortality and years of life lost (YLLs) from 288 causes of death by age-sex-location-year in 204 countries and territories and 811 subnational locations for each year from 1990 until 2021. The analysis used 56 604 data sources, including data from vital registration and verbal autopsy as well as surveys, censuses, surveillance systems, and cancer registries, among others. As with previous GBD rounds, cause-specific death rates for most causes were estimated using the Cause of Death Ensemble model-a modelling tool developed for GBD to assess the out-of-sample predictive validity of different statistical models and covariate permutations and combine those results to produce cause-specific mortality estimates-with alternative strategies adapted to model causes with insufficient data, substantial changes in reporting over the study period, or unusual epidemiology. YLLs were computed as the product of the number of deaths for each cause-age-sex-location-year and the standard life expectancy at each age. As part of the modelling process, uncertainty intervals (UIs) were generated using the 2·5th and 97·5th percentiles from a 1000-draw distribution for each metric. We decomposed life expectancy by cause of death, location, and year to show cause-specific effects on life expectancy from 1990 to 2021. We also used the coefficient of variation and the fraction of population affected by 90% of deaths to highlight concentrations of mortality. Findings are reported in counts and age-standardised rates. Methodological improvements for cause-of-death estimates in GBD 2021 include the expansion of under-5-years age group to include four new age groups, enhanced methods to account for stochastic variation of sparse data, and the inclusion of COVID-19 and other pandemic-related mortality-which includes excess mortality associated with the pandemic, excluding COVID-19, lower respiratory infections, measles, malaria, and pertussis. For this analysis, 199 new country-years of vital registration cause-of-death data, 5 country-years of surveillance data, 21 country-years of verbal autopsy data, and 94 country-years of other data types were added to those used in previous GBD rounds. FINDINGS The leading causes of age-standardised deaths globally were the same in 2019 as they were in 1990; in descending order, these were, ischaemic heart disease, stroke, chronic obstructive pulmonary disease, and lower respiratory infections. In 2021, however, COVID-19 replaced stroke as the second-leading age-standardised cause of death, with 94·0 deaths (95% UI 89·2-100·0) per 100 000 population. The COVID-19 pandemic shifted the rankings of the leading five causes, lowering stroke to the third-leading and chronic obstructive pulmonary disease to the fourth-leading position. In 2021, the highest age-standardised death rates from COVID-19 occurred in sub-Saharan Africa (271·0 deaths [250·1-290·7] per 100 000 population) and Latin America and the Caribbean (195·4 deaths [182·1-211·4] per 100 000 population). The lowest age-standardised death rates from COVID-19 were in the high-income super-region (48·1 deaths [47·4-48·8] per 100 000 population) and southeast Asia, east Asia, and Oceania (23·2 deaths [16·3-37·2] per 100 000 population). Globally, life expectancy steadily improved between 1990 and 2019 for 18 of the 22 investigated causes. Decomposition of global and regional life expectancy showed the positive effect that reductions in deaths from enteric infections, lower respiratory infections, stroke, and neonatal deaths, among others have contributed to improved survival over the study period. However, a net reduction of 1·6 years occurred in global life expectancy between 2019 and 2021, primarily due to increased death rates from COVID-19 and other pandemic-related mortality. Life expectancy was highly variable between super-regions over the study period, with southeast Asia, east Asia, and Oceania gaining 8·3 years (6·7-9·9) overall, while having the smallest reduction in life expectancy due to COVID-19 (0·4 years). The largest reduction in life expectancy due to COVID-19 occurred in Latin America and the Caribbean (3·6 years). Additionally, 53 of the 288 causes of death were highly concentrated in locations with less than 50% of the global population as of 2021, and these causes of death became progressively more concentrated since 1990, when only 44 causes showed this pattern. The concentration phenomenon is discussed heuristically with respect to enteric and lower respiratory infections, malaria, HIV/AIDS, neonatal disorders, tuberculosis, and measles. INTERPRETATION Long-standing gains in life expectancy and reductions in many of the leading causes of death have been disrupted by the COVID-19 pandemic, the adverse effects of which were spread unevenly among populations. Despite the pandemic, there has been continued progress in combatting several notable causes of death, leading to improved global life expectancy over the study period. Each of the seven GBD super-regions showed an overall improvement from 1990 and 2021, obscuring the negative effect in the years of the pandemic. Additionally, our findings regarding regional variation in causes of death driving increases in life expectancy hold clear policy utility. Analyses of shifting mortality trends reveal that several causes, once widespread globally, are now increasingly concentrated geographically. These changes in mortality concentration, alongside further investigation of changing risks, interventions, and relevant policy, present an important opportunity to deepen our understanding of mortality-reduction strategies. Examining patterns in mortality concentration might reveal areas where successful public health interventions have been implemented. Translating these successes to locations where certain causes of death remain entrenched can inform policies that work to improve life expectancy for people everywhere. FUNDING Bill & Melinda Gates Foundation
Therapeutic targets for malignant peripheral nerve sheath tumors
- Publication venue
- 'Future Medicine Ltd'
- Publication date
- Field of study
Zeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- Author
- Publication venue
- Nature America Inc.
- Publication date
- 01/01/2016
- Field of study
The mechanisms that coordinate and balance a complex network of opposing regulators to control Schwann cell (SC) differentiation remain elusive. Here we demonstrate that zinc-finger E-box-binding homeobox 2 (Zeb2, also called Sip1) transcription factor is a critical intrinsic timer that controls the onset of SC differentiation by recruiting histone deacetylases HDAC 1 and 2 (HDAC1/2) and nucleosome remodeling and deacetylase complex (NuRD) co-repressor complexes in mice. Zeb2 deletion arrests SCs at an undifferentiated state during peripheral nerve development and inhibits remyelination after injury. Zeb2 antagonizes inhibitory effectors including Notch and Sox2. Importantly, genome-wide transcriptome analysis reveals a Zeb2 target gene encoding the Notch effector Hey2 as a potent inhibitor for Schwann cell differentiation. Strikingly, a genetic Zeb2 variant associated with Mowat-Wilson syndrome disrupts the interaction with HDAC1/2-NuRD and abolishes Zeb2 activity for SC differentiation. Therefore, Zeb2 controls SC maturation by recruiting HDAC1/2-NuRD complexes and inhibiting a Notch-Hey2 signaling axis, pointing to the critical role of HDAC1/2-NuRD activity in peripheral neuropathies caused by ZEB2 mutations.status: publishe
Zeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/08/2016
- Field of study
The mechanisms that coordinate and balance a complex network of opposing regulators to control Schwann cell (SC) differentiation remain elusive. Here we demonstrate that zinc-finger E-box-binding homeobox 2 (Zeb2, also called Sip1) transcription factor is a critical intrinsic timer that controls the onset of SC differentiation by recruiting histone deacetylases HDAC 1 and 2 (HDAC1/2) and nucleosome remodeling and deacetylase complex (NuRD) co-repressor complexes in mice. Zeb2 deletion arrests SCs at an undifferentiated state during peripheral nerve development and inhibits remyelination after injury. Zeb2 antagonizes inhibitory effectors including Notch and Sox2. Importantly, genome-wide transcriptome analysis reveals a Zeb2 target gene encoding the Notch effector Hey2 as a potent inhibitor for Schwann cell differentiation. Strikingly, a genetic Zeb2 variant associated with Mowat-Wilson syndrome disrupts the interaction with HDAC1/2-NuRD and abolishes Zeb2 activity for SC differentiation. Therefore, Zeb2 controls SC maturation by recruiting HDAC1/2-NuRD complexes and inhibiting a Notch-Hey2 signaling axis, pointing to the critical role of HDAC1/2-NuRD activity in peripheral neuropathies caused by ZEB2 mutations.status: publishe